No abstract

A microscopic analysis of the morphology and ultrastructure of the digestive, salivary, and reproductive systems of adult Bemisia tabaci (Gennadius) (Hemiptera: Aleyrodidae) B type was conducted using light, scanning, and transmission electron microscopy. The internal anatomy of B. tabaci was found to be similar to that reported for Trialeurodes vaporariorum. In a microscopic analysis of the salivary glands, we have shown that each primary salivary gland is composed of at least 13 cells varying in morphology and staining differentially, while the accessory salivary glands are composed of four morphologically similar cells. We analyzed the course of the alimentary canal in B. tabaci, demonstrated the internal morphology of the organs, and clarified the location of the filter chamber relative to other organs in the whitefly. Our observations confirm that the pair of structures extending from the connecting chamber are caeca that may aid in fluid movement through the midgut and are not Malpighian tubules, as previously suggested. We confirm an earlier finding that the whitefly lacks Malpighian tubules, having instead specialized Malpighian-like cells within the filter chamber at the juncture with the internal ileum. Finally, we provide the first scanning electron microscopic analysis showing the reproductive organs of B. tabaci. Our investigation provides clarified terminology for several components of the digestive and excretory system. We also provide drawings and micrographs that will aid future researchers in localizing the internal organs of B. tabaci. We expect our analysis to provide a valuable tool for studying B. tabaci / plant virus interactions and physiological and biological aspects of this insect.

Interactions between viral and cellular membrane fusion proteins mediate virus penetration of cells for many arthropod-borne viruses. Electron microscope observations and circumstantial evidence indicate insect acquisition of tomato spotted wilt virus (TSWV) (genus Tospovirus, family Bunyaviridae) is receptor mediated, and TSWV membrane glycoproteins (GP1 and GP2) serve as virus attachment proteins. The tospoviruses are plant-infecting members of the family Bunyaviridae and are transmitted by several thrips species, including Frankliniella occidentalis. Gel overlay assays and immunolabeling were used to investigate the putative role of TSWV GPs as viral attachment proteins and deter mine whether a corresponding cellular receptor may be present in F. occidentalis. A single band in the 50-kDa region was detected with murine monoclonal antibodies (MAbs) to the TSWV-GPs when isolated TSWV or TSWV-GPs were used to overlay separated thrips proteins. This band was not detected when blots were probed with antibody to the non-structural protein encoded by the small RNA of TSWV or the TSWV nucleocapsid protein, nor were proteins from nonvector insects labeled. Anti-idiotype antibodies prepared to murine MAbs against GP1 or GP2 specifically labeled a single band at 50 kDa in Western blots and the plasmalemma of larval thrips midguts. These results support the putative role of the TSWV GPs as viral attachment proteins and identified potential cellular receptor(s) in thrips.

Aphis glycines Matsumura (Hemiptera: Aphididae), the soybean aphid, has become an important pest of soybeans, leading to significant yield losses in the United States. Host plant resistance is a viable alternative for managing A. glycines. The objectives of this study were to identify and categorize sources of resistance in soybean to A. glycines on genotypes from the United States and Brazil. An antixenosis assay was initially conducted with 8 genotypes to evaluate attractiveness to A. glycines. The selected soybean genotypes were further evaluated in a colonization assay to investigate the resistance of the genotypes at V1 (fully developed leaves at unifoliate node, 1st trifoliate leaf unrolled) and V3 (fully developed leaf at 2nd trifoliate node, 3rd trifoliate leaf unrolled) stages. An antibiosis assay was also conducted, in which multiple biological parameters of A. glycines were recorded. In the antixenosis assay, PI 200538, IAC 24, and IAC 17 genotypes were least attractive to adults of A. glycines, indicating moderate levels of antixenosis. The colonization assay showed that genotypes infested at the V3 stage had greater resistance when compared with the respective plants infested at the V1 stage. In addition, high levels of antibiosis to A. glycines were found in UX 2569-159, PI 200538, and PI 243540 genotypes. The identification of soybeans with resistance to A. glycines is of importance for the integrated pest management of this insect pest in the United States. Moreover, this research represents the first report on potential sources of resistance to A. glycines in soybeans from Brazil.

We report on the molecular, biochemical, and functional characterization of Cucurbita maxima phloem serpin-1 (CmPS-1), a novel 42-kDa serine proteinase inhibitor that is developmentally regulated and has antielastase properties. CmPS-1 was purified to near homogeneity from C. maxima (pumpkin) phloem exudate and, based on microsequence analysis, the cDNA encoding CmPS-1 was cloned. The association rate constant (k a ) of phloem-purified and recombinant His 6 -tagged CmPS-1 for elastase was 3.5 ؎ 1.6 ؋ 10 5 and 2.7 ؎ 0. with a 3:2 molar ratio. In vivo feeding assays conducted with the piercing-sucking aphid, Myzus persicae, established a close correlation between the developmentally regulated increase in CmPS-1 within the phloem sap and the reduced ability of these insects to survive and reproduce on C. maxima. However, in vitro feeding experiments, using purified phloem CmPS-1, failed to demonstrate a direct effect on aphid survival. Likely roles of this novel phloem serpin in defense against insects/ pathogens are discussed.The phloem long-distance translocation system of plants appears to function both as a nutrient delivery system and as an information superhighway (1-3). A central role for the phloem in the translocation of nutrients has long been recognized. The presence of plant hormones in the phloem sap (4, 5) implicated this long-distance transport pathway in the delivery of signaling molecules. Recent studies provided new insights into the nature of the information molecules being transported from mature leaves, via the phloem, to distant plant organs. Irrefutable evidence has been obtained for the translocation of certain proteins (6 -9). In addition, it has also been demonstrated that specific RNA molecules are present in the phloem sap (10, 11) and some move to distant tissues, where they appear to influence post-transcriptional events (9, 12).Given the importance of this nutrient/information delivery system to the functioning of the plant, it was axiomatic that plants had to evolve mechanisms to protect the operational integrity of the phloem. Maintenance of structural integrity required the development of systems able to rapidly respond to physical damage, imposed either by environmental forces or herbivory; the sealing of disrupted sieve tubes involves deposition of material at the level of the sieve plate pore (1). In the enucleate sieve tube system of angiosperms, maintenance of membrane integrity has also been transferred to the neighboring companion cells and likely involves the delivery of essential constituents via plasmodesmata (6,13,14).To ensure the integrity of the signaling components, the plant needs also to protect against protein and RNA degradation occurring within the phloem sap. This capacity appears to have been achieved through the development of a control system that regulates the plasmodesmal-mediated exchange of macromolecules between companion cells and the sieve tube system (9, 12, 13). The absence of proteinase activity (15) within the phloem sap is consistent with this mo...